Dipropylamine → HCID 10456143, compound
Reaction equation
Br[CH2:2][C:3](Br)=[O:4].[CH2:6]([NH:9][CH2:10][CH2:11][CH3:12])[CH2:7][CH3:8].[C:13]([C:17]1[CH:22]=[CH:21][C:20]([S:23]([NH:26][C:27]2[CH:32]=[CH:31][C:30]([CH3:33])=[CH:29][CH:28]=2)(=[O:25])=[O:24])=[CH:19][CH:18]=1)([CH3:16])([CH3:15])[CH3:14]>>[C:13]([C:17]1[CH:18]=[CH:19][C:20]([S:23]([N:26]([C:27]2[CH:28]=[CH:29][C:30]([CH3:33])=[CH:31][CH:32]=2)[CH2:2][C:3]([N:9]([CH2:10][CH2:11][CH3:12])[CH2:6][CH2:7][CH3:8])=[O:4])(=[O:25])=[O:24])=[CH:21][CH:22]=1)([CH3:16])([CH3:15])[CH3:14]Participants
4
Procedure
prepared by reaction of 2-bromoacetyl bromide with di-n-propylamine and 4-tert-butyl-N-p-tolyl-benzenesulfonamide
Sources & evidence
- ORD record
- ord-0c006354154848eab68cfb235cd8153d
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07435815B2
Reaction notes
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